References
- Meyer JD, Manning MC. (1998). Hydrophobic ion pairing: altering the solubility properties of biomolecules. Pharm Res, 15, 188–93.
- Khutoryanskiy VV (2007). Hydrogen-bonded interpolymer complexes as materials for pharmaceutical applications. Int J Pharm, 334, 15–26.
- Khutoryanskiy VV, Dubolazov AV, Nurkeeva ZS, Mun GA. (2004). PH effects in the complex formation and blending of poly(acrylic acid) with poly(ethylene oxide). Langmuir, 20, 3785–90.
- Bailey FE, Lundberg RD, Callard RW. (1964). Some factors affecting the molecular association of poly(ethylene oxide) and poly(acrylic acid) in aqueous solution. J Polym Sci Part A, 2, 845–51.
- Ikawa T, Abe K., Honda K, Tsuchida E. (1975). Interpolymer complex between poly (ethylene oxide) and poly (acrylic acid). J Polym Sci Chem A, 13, 1505–14.
- Choi SH, Park TG. (2000). Hydrophobic ion pair formation between leuprolide and sodium oleate for sustained release from biodegradable polymeric microspheres. Int J Pharm, 203, 193–202.
- Yuan H, Jiang SP, Du YZ, Miao J, Zhang XG, Hu FQ. (2009). Strategic approaches for improving entrapment of hydrophilic peptide drugs by lipid nanoparticles - Colloids Surf. B. Biointerfaces, 70, 248–53.
- Shi K, Cui F, Yamamoto H, Kawashima Y. (2008). Investigation of drug loading and in vitro release mechanisms of insulin-lauryl sulfate complex loaded PLGA nanoparticles. Pharmazie, 63, 866–71.
- Shi K, Cui F, Yamamoto H, Kawashima Y. (2008). Optimized preparation of insulin-lauryl sulfate complex loaded poly (lactide-co-glycolide) nanoparticles using response surface methodology. Pharmazie, 63, 721–25.
- Deutel B, Greindl M, Thaurer M, Bernkop-Schnurch A. (2008). Novel insulin thiomer nanoparticles: in vivo evaluation of an oral drug delivery system. Biomacromolecules, 9, 278–85.
- Perera G, Greindl M, Palmberger TF, Bernkop-Schnurch A. (2009). Insulin-loaded poly(acrylic acid)-cysteine nanoparticles: stability studies towards digestive enzymes of the intestine. Drug Deliv, 16, 254–60.
- Chun MK, Cho CS, Choi HK. (2002). Mucoadhesive drug carrier based on interpolymer complex of poly(vinyl pyrrolidone) and poly(acrylic acid) prepared by template polymerization. J Control Release, 81, 327–34.
- Arakawa T, Philo J, Kenney WC. (1994). Structure and solubility of interleukin-2 in sodium dodecyl sulfate. Int J Pept Protein Res, 43, 583–87.
- Aungst BJ, Hussain MA. (1992). Sustained propranolol delivery and increased oral bioavailability in dogs given a propranolol Laurate salt. Pharm Res, 9, 1507–09.
- Mcshane MM, Kruske CA, Davio SR, Wilkinson KF, Rush BD, Ruwart MJ. (1994). The effect of aqueous solubility on the absorption of peptide-like drugs from the subcutaneous (SC) site. Pharm Res, 11, S–246.
- Trimble K, Wan J, Floy B. (1993). Effects of ion pairing agents on partition coefficient, tissue uptake, and membrane permeability of LHRH analogues - Pharm Res, 10, S–178.
- Delie F, Blanco-Prieto MJ. (2005). Polymeric particulates to improve oral bioavailability of peptide drugs. Molecules. 10, 65–80.
- Chun MK, Cho CS, Choi HK. (2001). A novel mucoadhesive polymer prepared by template polymerization of acrylic acid in the presence of poloxamer. J App Polym Sci, 79, 1525–30.
- Younessi P, Avadi MR, Shamimi K, Sadeghi AM, Moezi L, Nahid E, Bayati K, Dehpour AR, Rafiee-Tehrani M. (2004). Preparation and ex vivo evaluation of TEC as an absorption enhancer for poorly absorbable compounds in colon specific drug delivery. Acta Pharm, 54, 339–45.